Genetic contributions to stuttering: the current evidence

A Mutation Associated with Stuttering Alters Mouse Pup Ultrasonic Vocalizations

(2016) Terra D. Barnes et al.   CURRENT BIOLOGY

Association between Rare Variants in AP4E1, a Component of Intracellular Trafficking, and Persistent Stuttering

(2015) M. Hashim Raza et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Mucolipidosis types II and III and non-syndromic stuttering are associated with different variants in the same genes

(2015) M Hashim Raza et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

A genetic linkage study in Brazil identifies a new locus for persistent developmental stuttering on chromosome 10

(2014) C.E.F. Domingues et al.   GENETICS AND MOLECULAR RESEARCH

Stuck in traffic: an emerging theme in diseases of the nervous system

(2014) Jacques Neefjes et al.   TRENDS IN NEUROSCIENCES

RAB7L1 Interacts with LRRK2 to Modify Intraneuronal Protein Sorting and Parkinson’s Disease Risk

(2013) David A. MacLeod et al.   NEURON

A Novel Homozygous p.R1105X Mutation of the AP4E1 Gene in Twins with Hereditary Spastic Paraplegia and Mycobacterial Disease

(2013) Xiao-Fei Kong et al.   PLoS One

Linkage analysis of a large African family segregating stuttering suggests polygenic inheritance

(2012) M. Hashim Raza et al.   HUMAN GENETICS

A role for inherited metabolic deficits in persistent developmental stuttering

(2012) Changsoo Kang et al.   MOLECULAR GENETICS AND METABOLISM

Genetic and environmental effects on stuttering: A twin study from Finland

(2012) Pirkko Rautakoski et al.   JOURNAL OF FLUENCY DISORDERS

Adaptor Protein Complex 4 Deficiency Causes Severe Autosomal-Recessive Intellectual Disability, Progressive Spastic Paraplegia, Shy Character, and Short Stature

(2011) Rami Abou Jamra et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Studies in a consanguineous family reveal a novel locus for stuttering on chromosome 16q

(2011) Muhammad Hashim Raza et al.   HUMAN GENETICS

Analysis of Mannose 6-Phosphate Uncovering Enzyme Mutations Associated with Persistent Stuttering

(2011) Wang-Sik Lee et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Cross Fostering Experiments Suggest That Mice Songs Are Innate

(2011) Takefumi Kikusui et al.   PLoS One

Sorting of the Alzheimer's Disease Amyloid Precursor Protein Mediated by the AP-4 Complex

(2010) Patricia V. Burgos et al.   DEVELOPMENTAL CELL

Identification of an autosomal recessive stuttering locus on chromosome 3q13.2–3q13.33

(2010) Muhammad Hashim Raza et al.   HUMAN GENETICS

Characterization of a mutation commonly associated with persistent stuttering: evidence for a founder mutation

(2010) Alison Fedyna et al.   JOURNAL OF HUMAN GENETICS

Adaptor protein complex-4 (AP-4) deficiency causes a novel autosomal recessive cerebral palsy syndrome with microcephaly and intellectual disability

(2010) A. Moreno-De-Luca et al.   JOURNAL OF MEDICAL GENETICS

Heritability and environmental effects for self-reported periods with stuttering: A twin study from Denmark

(2010) Corrado Fagnani et al.   Logopedics Phoniatrics Vocology

Mutations in the Lysosomal Enzyme–Targeting Pathway and Persistent Stuttering

(2010) Changsoo Kang et al.   NEW ENGLAND JOURNAL OF MEDICINE

Huntingtin as an essential integrator of intracellular vesicular trafficking

(2009) Juliane P. Caviston et al.   TRENDS IN CELL BIOLOGY

Bivariate Genetic Analyses of Stuttering and Nonfluency in a Large Sample of 5-Year-Old Twins

(2009) Catharina Eugenie Maria van Beijsterveldt et al.   JOURNAL OF SPEECH LANGUAGE AND HEARING RESEARCH

Accumulation of AMPA Receptors in Autophagosomes in Neuronal Axons Lacking Adaptor Protein AP-4

(2008) Shinji Matsuda et al.   NEURON